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HRID 1506438作成日:2026年10月26日

Hydroxyamine hydrochloride → (NE)-N-[[4-bromo-2-[3-[5-phenyl-4-(trifluoromethyl)-1,2-oxazol-3-yl]prop-2-ynoxy]phenyl]methylidene]hydroxylamine

https://huagongshe.com/reaction/1506438

反応式

関与物質

役割名称HCID仕込み量
反応物Hydroxyamine hydrochlorideHCID 443297—
反応物Sodium AcetateHCID 517045—
反応物4-Bromo-2-(3-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)prop-2-ynyloxy)benzaldehydeHCID 86669907—
溶媒MethanolHCID 887—
生成物(NE)-N-[[4-bromo-2-[3-[5-phenyl-4-(trifluoromethyl)-1,2-oxazol-3-yl]prop-2-ynoxy]phenyl]methylidene]hydroxylamineHCID 8729407097%

反応手順

A mixture of 4-bromo-2-(3-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)prop-2-ynyloxy)benzaldehyde (Preparation 62D, 0.050 g, 0.111 mmol), hydroxylamine hydrochloride (9.26 mg, 0.133 mmol), and sodium acetate (0.018 g, 0.222 mmol) in methanol (2.0 mL) was heated at reflux for 30 min. The solvent was removed under reduce pressure, and the residue was diluted with dichloromethane, washed with water, and dried over anhydrous sodium sulfate. Concentration under reduced pressure afforded (E)-4-bromo-2-(3-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)prop-2-ynyloxy)benzaldehyde oxime (0.050 g, 0.107 mmol, 97% yield) as a white solid. The product had an HPLC with a ret. time=3.26 min.−Column: Chromolith SpeedROD 4.6×50 mm (4 min.); Solvent A=10% MeOH, 90% H2O, 0.1% TFA; Solvent B=90% MeOH, 10% H2O, 0.1% TFA. LC/MS M+1=466.8.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09216972B2
出典データセットuspto-grants-2015_12
ORD IDord-94b3a796633f4bb38f1b5aa9560f9d56
出典メモuspto-grants-2015_12